Senior Backend Developer

Descripción del trabajo

I am working with a highly innovative biotech company based in Barcelona, specializing in the development of groundbreaking medical devices. We are looking for a Regulatory Affairs & Quality Assurance Specialist to join their team.

Ideal Profile:

• Experience in regulatory strategies and documentation preparation for CE Marking and FDA submissions.
• Implementation of Quality Management Systems (ISO 13485, MDR).
• Project management in Class IIa medical devices.

What the Role Offers:

• The opportunity to be part of a biotech company developing high-impact medical technology for cardiovascular disease prevention.
• Hybrid work model (remote / in-office in Barcelona).
• A dynamic and innovative environment with a competitive salary.